Cargando…
CAR T-cell therapy for B-cell lymphomas: clinical trial results of available products
Adoptive cellular immunotherapy with chimeric antigen receptor (CAR) T cell has changed the treatment landscape of B-cell non-Hodgkin’s lymphoma (NHL), especially for aggressive B-cell lymphomas. Single-center and multicenter clinical trials with anti-CD19 CAR T-cell therapy have shown great activit...
Autores principales: | , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
SAGE Publications
2019
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6466472/ https://www.ncbi.nlm.nih.gov/pubmed/31019670 http://dx.doi.org/10.1177/2040620719841581 |
_version_ | 1783411117068910592 |
---|---|
author | Chavez, Julio C. Bachmeier, Christina Kharfan-Dabaja, Mohamed A. |
author_facet | Chavez, Julio C. Bachmeier, Christina Kharfan-Dabaja, Mohamed A. |
author_sort | Chavez, Julio C. |
collection | PubMed |
description | Adoptive cellular immunotherapy with chimeric antigen receptor (CAR) T cell has changed the treatment landscape of B-cell non-Hodgkin’s lymphoma (NHL), especially for aggressive B-cell lymphomas. Single-center and multicenter clinical trials with anti-CD19 CAR T-cell therapy have shown great activity and long-term remissions in poor-risk diffuse large B-cell lymphoma (DLBCL) when no other effective treatment options are available. Two CAR T-cell products [axicabtagene ciloleucel (axi-cel) and tisagenlecleucel] have obtained US Food and Drug Administration approval for the treatment of refractory DLBCL after two lines of therapy. A third product, liso-cel, is currently being evaluated in clinical trials and preliminary results appear very promising. CAR T-cell-related toxicity with cytokine-release syndrome and neurotoxicity remain important potential complications of this therapy. Here, we review the s biology, structure, clinical trial results and toxicity of two commercially approved CAR T-cell products and others currently being studied in multicenter clinical trials in B-cell NHLs. |
format | Online Article Text |
id | pubmed-6466472 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | SAGE Publications |
record_format | MEDLINE/PubMed |
spelling | pubmed-64664722019-04-24 CAR T-cell therapy for B-cell lymphomas: clinical trial results of available products Chavez, Julio C. Bachmeier, Christina Kharfan-Dabaja, Mohamed A. Ther Adv Hematol Review Adoptive cellular immunotherapy with chimeric antigen receptor (CAR) T cell has changed the treatment landscape of B-cell non-Hodgkin’s lymphoma (NHL), especially for aggressive B-cell lymphomas. Single-center and multicenter clinical trials with anti-CD19 CAR T-cell therapy have shown great activity and long-term remissions in poor-risk diffuse large B-cell lymphoma (DLBCL) when no other effective treatment options are available. Two CAR T-cell products [axicabtagene ciloleucel (axi-cel) and tisagenlecleucel] have obtained US Food and Drug Administration approval for the treatment of refractory DLBCL after two lines of therapy. A third product, liso-cel, is currently being evaluated in clinical trials and preliminary results appear very promising. CAR T-cell-related toxicity with cytokine-release syndrome and neurotoxicity remain important potential complications of this therapy. Here, we review the s biology, structure, clinical trial results and toxicity of two commercially approved CAR T-cell products and others currently being studied in multicenter clinical trials in B-cell NHLs. SAGE Publications 2019-04-15 /pmc/articles/PMC6466472/ /pubmed/31019670 http://dx.doi.org/10.1177/2040620719841581 Text en © The Author(s), 2019 http://www.creativecommons.org/licenses/by-nc/4.0/ This article is distributed under the terms of the Creative Commons Attribution-NonCommercial 4.0 License (http://www.creativecommons.org/licenses/by-nc/4.0/) which permits non-commercial use, reproduction and distribution of the work without further permission provided the original work is attributed as specified on the SAGE and Open Access pages (https://us.sagepub.com/en-us/nam/open-access-at-sage). |
spellingShingle | Review Chavez, Julio C. Bachmeier, Christina Kharfan-Dabaja, Mohamed A. CAR T-cell therapy for B-cell lymphomas: clinical trial results of available products |
title | CAR T-cell therapy for B-cell lymphomas: clinical trial results of
available products |
title_full | CAR T-cell therapy for B-cell lymphomas: clinical trial results of
available products |
title_fullStr | CAR T-cell therapy for B-cell lymphomas: clinical trial results of
available products |
title_full_unstemmed | CAR T-cell therapy for B-cell lymphomas: clinical trial results of
available products |
title_short | CAR T-cell therapy for B-cell lymphomas: clinical trial results of
available products |
title_sort | car t-cell therapy for b-cell lymphomas: clinical trial results of
available products |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6466472/ https://www.ncbi.nlm.nih.gov/pubmed/31019670 http://dx.doi.org/10.1177/2040620719841581 |
work_keys_str_mv | AT chavezjulioc cartcelltherapyforbcelllymphomasclinicaltrialresultsofavailableproducts AT bachmeierchristina cartcelltherapyforbcelllymphomasclinicaltrialresultsofavailableproducts AT kharfandabajamohameda cartcelltherapyforbcelllymphomasclinicaltrialresultsofavailableproducts |